Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: RGS1[original query] |
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Six new coeliac disease loci replicated in an Italian population confirm association with coeliac disease. Journal of medical genetics 2009 Jan 46 (1): 60-3. Romanos J, Barisani D, Trynka G, Zhernakova A, Bardella M T, Wijmenga |
Newly identified genetic risk variants for celiac disease related to the immune response.
Nature genetics 2008 Apr 40 (4): 395-402. Hunt Karen A, Zhernakova Alexandra, Turner Graham, Heap Graham A R, Franke Lude, Bruinenberg Marcel, Romanos Jihane, Dinesen Lotte C, Ryan Anthony W, Panesar Davinder, Gwilliam Rhian, Takeuchi Fumihiko, McLaren William M, Holmes Geoffrey K T, Howdle Peter D, Walters Julian R F, Sanders David S, Playford Raymond J, Trynka Gosia, Mulder Chris J J, Mearin M Luisa, Verbeek Wieke H M, Trimble Valerie, Stevens Fiona M, O'Morain Colm, Kennedy Nicholas P, Kelleher Dermot, Pennington Daniel J, Strachan David P, McArdle Wendy L, Mein Charles A, Wapenaar Martin C, Deloukas Panos, McGinnis Ralph, McManus Ross, Wijmenga Cisca, van Heel David |
Shared and distinct genetic variants in type 1 diabetes and celiac disease. The New England journal of medicine 2008 Dec 359 (26): 2767-77. Smyth Deborah J, Plagnol Vincent, Walker Neil M, Cooper Jason D, Downes Kate, Yang Jennie H M, Howson Joanna M M, Stevens Helen, McManus Ross, Wijmenga Cisca, Heap Graham A, Dubois Patrick C, Clayton David G, Hunt Karen A, van Heel David A, Todd John |
Four novel coeliac disease regions replicated in an association study of a Swedish-Norwegian family cohort. Genes and immunity 2010 Jan 11 (1): 79-86. Amundsen S S, Rundberg J, Adamovic S, Gudjónsdóttir A H, Ascher H, Ek J, Nilsson S, Lie B A, Naluai A T, Sollid L |
Multiple sclerosis susceptibility alleles in African Americans. Genes and immunity 2010 Jun 11 (4): 343-50. Johnson B A, Wang J, Taylor E M, Caillier S J, Herbert J, Khan O A, Cross A H, De Jager P L, Gourraud P-A F, Cree B C A, Hauser S L, Oksenberg J |
Genome-wide analysis of chromosomal alterations in patients with esophageal squamous cell carcinoma exposed to tobacco and betel quid from high-risk area in India. Mutation research 2010 Feb 696 (2): 130-8. Chattopadhyay Indranil, Singh Avninder, Phukan Rupkumar, Purkayastha Joydeep, Kataki Amal, Mahanta Jagadish, Saxena Sunita, Kapur Suja |
Genetic variations in the regulator of G-protein signaling genes are associated with survival in late-stage non-small cell lung cancer. PloS one 2011 6 (6): 6. Dai J, Gu J, Lu C, Lin J, Stewart D, Chang D, Roth JA, Wu X |
Revisiting genome wide association studies (GWAS) in coeliac disease: replication study in Spanish population and expression analysis of candidate genes. Journal of medical genetics 2011 Jul 48 (7): 493-6. Plaza-Izurieta Leticia, Castellanos-Rubio Ainara, Irastorza Iñaki, Fernández-Jimenez Nora, Gutierrez Galder, , Bilbao Jose Ram |
Improving the estimation of celiac disease sibling risk by non-HLA genes. PloS one 2011 6 (11): e26920. Izzo Valentina, Pinelli Michele, Tinto Nadia, Esposito Maria Valeria, Cola Arturo, Sperandeo Maria Pia, Tucci Francesca, Cocozza Sergio, Greco Luigi, Sacchetti Luc |
Multiple sclerosis risk genotypes correlate with an elevated cerebrospinal fluid level of the suggested prognostic marker CXCL13. Multiple sclerosis (Houndmills, Basingstoke, England) 2013 Jun 19 (7): 863-70. Lindén M, Khademi M, Lima Bomfim I, Piehl F, Jagodic M, Kockum I, Olsson |
Inherited variants in regulatory T cell genes and outcome of ovarian cancer. PloS one 2013 8 (1): 1. Goode EL, Derycke M, Kalli KR, Oberg AL, Cunningham JM, Maurer MJ, Fridley BL, Armasu SM, Serie DJ, Ramar P, Goergen K, Vierkant RA, Rider DN, Sicotte H, Wang C, Winterhoff B, Phelan CM, Schildkraut JM, Weber RP, Iversen E, Berchuck A, Sutphen R, Birrer MJ, Hampras S, Preus L, Gayther SA, Ramus SJ, Wentzensen N, Yang HP, Garcia-Closas M, Song H, Tyrer J, Pharoah PP, Konecny G, Sellers TA, Ness RB, Sucheston LE, Odunsi K, Hartmann LC, Moysich KB, Knutson KL |
Clinical relevance and functional consequences of the TNFRSF1A multiple sclerosis locus. Neurology 2013 Nov 81 (22): 1891-9. Ottoboni Linda, Frohlich Irene Y, Lee Michelle, Healy Brian C, Keenan Brendan T, Xia Zongqi, Chitnis Tanuja, Guttmann Charles R, Khoury Samia J, Weiner Howard L, Hafler David A, De Jager Philip |
Multiple sclerosis susceptibility genes: associations with relapse severity and recovery. PloS one 2013 8 (10): e75416. Mowry Ellen M, Carey Robert F, Blasco Maria R, Pelletier Jean, Duquette Pierre, Villoslada Pablo, Malikova Irina, Roger Elaine, Kinkel R Phillip, McDonald Jamie, Bacchetti Peter, Waubant Emmanuel |
Genetic association between RGS1 and internalizing disorders. Psychiatric genetics 2013 Apr 23 (2): 56-60. Hettema John M, An Seon-Sook, van den Oord Edwin J C G, Neale Michael C, Kendler Kenneth S, Chen Xiangni |
Dense genotyping of immune-related loci in idiopathic inflammatory myopathies confirms HLA alleles as the strongest genetic risk factor and suggests different genetic background for major clinical subgroups.
Annals of the rheumatic diseases 2015 Sep . Rothwell Simon, Cooper Robert G, Lundberg Ingrid E, Miller Frederick W, Gregersen Peter K, Bowes John, Vencovsky Jiri, Danko Katalin, Limaye Vidya, Selva-O'Callaghan Albert, Hanna Michael G, Machado Pedro M, Pachman Lauren M, Reed Ann M, Rider Lisa G, Cobb Joanna, Platt Hazel, Molberg Øyvind, Benveniste Olivier, Mathiesen Pernille, Radstake Timothy, Doria Andrea, De Bleecker Jan, De Paepe Boel, Maurer Britta, Ollier William E, Padyukov Leonid, O'Hanlon Terrance P, Lee Annette, Amos Christopher I, Gieger Christian, Meitinger Thomas, Winkelmann Juliane, Wedderburn Lucy R, Chinoy Hector, Lamb Janine A, |
Anti-inflammatory genes associated with multiple sclerosis: a gene expression study. Journal of neuroimmunology 2015 Feb 279 75-8. Perga S, Montarolo F, Martire S, Berchialla P, Malucchi S, Bertolotto |
New candidates for CD4 T cell pathogenicity in experimental neuroinflammation and multiple sclerosis. Brain : a journal of neurology 2015 Apr 138 (Pt 4): 902-17. Hoppmann Nicola, Graetz Christiane, Paterka Magdalena, Poisa-Beiro Laura, Larochelle Catherine, Hasan Maruf, Lill Christina M, Zipp Frauke, Siffrin Volk |
Multiple sclerosis risk loci correlate with cervical cord atrophy and may explain the course of disability. Neurogenetics 2015 Jul 16 (3): 161-8. Akkad Denis A, Bellenberg Barbara, Esser Sarika, Weiler Florian, Epplen Jörg T, Gold Ralf, Lukas Carsten, Haghikia Aid |
Meta-Analysis on Associations of RGS1 and IL12A Polymorphisms with Celiac Disease Risk. International journal of molecular sciences 2016 17 (4): . Guo Cong-Cong, Wang Man, Cao Feng-Di, Huang Wei-Huang, Xiao Di, Ye Xing-Guang, Ou Mei-Ling, Zhang Na, Zhang Bao-Huan, Liu Yang, Yang Guang, Jing Chun-X |
Novel identified associations of RGS1 and RASGRP1 variants in IgA Nephropathy. Scientific reports 2016 Nov 6 35781. Zhou Xu-Jie, Nath Swapan K, Qi Yuan-Yuan, Sun Celi, Hou Ping, Zhang Yue-Miao, Lv Ji-Cheng, Shi Su-Fang, Liu Li-Jun, Chen Ruoyan, Yang Wanling, He Kevin Zhi, Li Yanming, Zhang Ho |
A human microglia-like cellular model for assessing the effects of neurodegenerative disease gene variants. Science translational medicine 2017 12 9 (421): . Ryan Katie J, White Charles C, Patel Kruti, Xu Jishu, Olah Marta, Replogle Joseph M, Frangieh Michael, Cimpean Maria, Winn Phoebe, McHenry Allison, Kaskow Belinda J, Chan Gail, Cuerdon Nicole, Bennett David A, Boyd Justin D, Imitola Jaime, Elyaman Wassim, De Jager Philip L, Bradshaw Elizabeth |
HLA and non-HLA genes and familial predisposition to autoimmune diseases in families with a child affected by type 1 diabetes. PloS one 2017 11 12 (11): e0188402. Parkkola Anna, Laine Antti-Pekka, Karhunen Markku, Härkönen Taina, Ryhänen Samppa J, Ilonen Jorma, Knip Mikael, |
Field Synopsis and Re-analysis of Systematic Meta-analyses of Genetic Association Studies in Multiple Sclerosis: a Bayesian Approach. Molecular neurobiology 2017 10 55 (7): 5672-5688. Park Jae Hyon, Kim Joo Hi, Jo Kye Eun, Na Se Whan, Eisenhut Michael, Kronbichler Andreas, Lee Keum Hwa, Shin Jae |
Replication study of GWAS risk loci in Greek multiple sclerosis patients. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2019 Feb 40 (2): 253-260. Hadjigeorgiou Georgios M, Kountra Persia-Maria, Koutsis Georgios, Tsimourtou Vana, Siokas Vasileios, Dardioti Maria, Rikos Dimitrios, Marogianni Chrysoula, Aloizou Athina-Maria, Karadima Georgia, Ralli Styliani, Grigoriadis Nikolaos, Bogdanos Dimitrios, Panas Marios, Dardiotis Efthimi |
Genetic Variants Associated With Neurodegenerative Diseases Regulate Gene Expression in Immune Cell CD14+ Monocytes. Frontiers in genetics 2019 1 9 666. Sun Jing-Yi, Hou Ya-Jun, Zhang Yan, Wang Longcai, Liu Lidong, Sun Bao-Liang, Yuan H |
Targeted resequencing reveals rare variants enrichment in multiple sclerosis susceptibility genes. Human mutation 2020 Mar . Gil-Varea Elia, Spataro Nino, Villar Luisa María, Tejeda-Velarde Amalia, Midaglia Luciana, Matesanz Fuencisla, Malhotra Sunny, Eixarch Herena, Patsopoulos Nikolaos, Fernández Óscar, Oliver-Martos Begoña, Saiz Albert, Llufriu Sara, Ramió-Torrentà Lluís, Quintana Ester, Izquierdo Guillermo, Alcina Antonio, Bosch Elena, Navarro Arcadi, Montalban Xavier, Comabella Manu |
Single-cell combined bioinformatics analysis: construction of immune cluster and risk prognostic model in kidney renal clear cells based on CD8 T cell-associated genes. European journal of medical research 2024 1 29 (1): 89. Haifeng Gao, Hang Sun, Aifeng He, Hui Liu, Zihang Zhang, Dongling Li, Weipu Mao, Jinke Qi |
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- Page last updated:Jun 03, 2024
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